Canonical Allele Identifier: CA2577536127

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30623143C>T , CM000665.2:g.30623143C>T	GRCh38
NC_000003.11:g.30664635C>T , CM000665.1:g.30664635C>T	GRCh37
NC_000003.10:g.30639639C>T	NCBI36
NG_007490.1:g.21642C>T , LRG_779:g.21642C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.94+16166C>T MANE Select	ENSP00000295754.5:n.94+16166C>T
ENST00000673250.1:n.144-56C>T
ENST00000295754.9:c.94+16166C>T	ENSP00000295754.5:n.94+16166C>T
ENST00000359013.4:c.95-56C>T	ENSP00000351905.4:n.95-56C>T
NM_001024847.2:c.95-56C>T , LRG_779t1:c.95-56C>T	NP_001020018.1:n.95-56C>T
NM_003242.5:c.94+16166C>T	NP_003233.4:n.94+16166C>T
XM_011534043.1:c.47-56C>T	XP_011532345.1:n.47-56C>T
XM_011534044.1:c.46+8437C>T	XP_011532346.1:n.46+8437C>T
XM_011534045.1:c.-12+16550C>T	XP_011532347.1:n.-12+16550C>T
XM_011534043.2:c.47-56C>T	XP_011532345.1:n.47-56C>T
XM_011534045.3:c.-12+16550C>T	XP_011532347.1:n.-12+16550C>T
NM_003242.6:c.94+16166C>T MANE Select	NP_003233.4:n.94+16166C>T